Identification of a physiological E2 module for the human anaphase-promoting complex

被引:234
|
作者
Williamson, Adam [1 ]
Wickliffe, Katherine E. [1 ]
Mellone, Barbara G. [1 ,2 ]
Song, Ling [1 ]
Karpen, Gary H. [1 ,2 ]
Rape, Michael [1 ]
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Lawrence Berkeley Lab, Dept Genome Dynam, Berkeley, CA 94720 USA
基金
美国国家卫生研究院;
关键词
K11-linked chain; proteasome; ubiquitin; SPINDLE ASSEMBLY CHECKPOINT; UBIQUITIN-LIKE PROTEINS; DEPENDENT PROTEOLYSIS; MITOTIC SPINDLE; CHAIN FORMATION; KEN BOX; DEGRADATION; APC; COMPLEX/CYCLOSOME; REVEALS;
D O I
10.1073/pnas.0907887106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Ubiquitination by the anaphase-promoting complex (APC/C) is essential for proliferation in all eukaryotes. The human APC/C promotes the degradation of mitotic regulators by assembling K11-linked ubiquitin chains, the formation of which is initiated by its E2 UbcH10. Here, we identify the conserved Ube2S as a K11-specific chain elongating E2 for human and Drosophila APC/C. Ube2S depends on the cell cycle-dependent association with the APC/C activators Cdc20 and Cdh1 for its activity. While depletion of Ube2S already inhibits APC/C in cells, the loss of the complete UbcH10/Ube2S-module leads to dramatic stabilization of APC/C substrates, severe spindle defects, and a strong mitotic delay. Ube2S and UbcH10 are tightly co-regulated in the cell cycle by APC/C-dependent degradation. We conclude that UbcH10 and Ube2S constitute a physiological E2-module for APC/C, the activity of which is required for spindle assembly and cell division.
引用
收藏
页码:18213 / 18218
页数:6
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